| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:53981403-53981681 | Common:1; Rare:45 | ||||
| chr16:54016316-54016534 | Common:1; Rare:28 | ||||
| chr16:55485273-55485776 | Common:2; Rare:146; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr16:55498283-55498573 | Common:1; Rare:79; Clinvar:2 | ||||
| chr16:55510289-55510914 | Common:5; Rare:115 | ||||
| chr16:55512154-55512391 | Common:1; Rare:32 | ||||
| chr16:55514577-55514607 | Rare:2 | ||||
| chr16:55514984-55515743 | Common:10; Rare:113 | ||||
| chr16:55516586-55516913 | Common:1; Rare:57 | ||||
| chr16:55517763-55517970 | Common:1; Rare:29 | ||||
| chr16:55518917-55519185 | Common:2; Rare:34 | ||||
| chr16:55519300-55519780 | Common:4; Rare:81 | ||||
| chr16:55520516-55520763 | Rare:39 | ||||
| chr16:55532676-55532847 | Rare:29 | ||||
| chr16:55538231-55538552 | Common:2; Rare:46 |